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Author Details
Full Name
Nephi Walton
Affiliation
Genomic Medicine Institute
ORCID
Career Start Year
2007
Papers
22
H Index
9
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36281494
Genetic testing and counseling for the unexplained epilepsies: An evidence-based practice guideline of the National Society of Genetic Counselors.
J Genet Couns
2023
37274607
Paving a pathway for large-scale utilization of genomics in precision medicine and population health.
Front Sociol
2023
36474423
Characterizing variability of electronic health record-driven phenotype definitions.
J Am Med Inform Assoc
2023
36737471
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.
Sci Rep
2023
35308907
Creating a Home for Genomic Data in the Electronic Health Record.
AMIA Annu Symp Proc
2022
35485600
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
J Am Med Inform Assoc
2022
36579594
The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population Health.
J Pers Med
2022
36372681
Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.
Obesity (Silver Spring)
2022
35090449
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC Med Inform Decis Mak
2022
33480803
Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hypercholesterolemia.
Circ Genom Precis Med
2021
34381794
Legal Challenges in Precision Medicine: What Duties Arising From Genetic and Genomic Testing Does a Physician Owe to Patients?
Front Med (Lausanne)
2021
33979874
Infobuttons for Genomic Medicine: Requirements and Barriers.
Appl Clin Inform
2021
32308829
Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.
AMIA Annu Symp Proc
2020
32696950
Infant acid suppression use is associated with the development of eosinophilic esophagitis.
Dis Esophagus
2020
30803986
Distal chromosome 16p11.2 duplications containing <i>SH2B1</i> in patients with scoliosis.
J Med Genet
2019
31737042
Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network.
Front Genet
2019
31297895
Future directions for high-throughput splicing assays in precision medicine.
Hum Mutat
2019
31258966
Comorbidity Characterization Among eMERGE Institutions: A Pilot Evaluation with the Johns Hopkins Adjusted Clinical Groups® System.
AMIA Jt Summits Transl Sci Proc
2019
28381817
The Complex Genetic Basis of Congenital Heart Defects.
Circ J
2017
21510889
Modeling the variations in pediatric respiratory syncytial virus seasonal epidemics.
BMC Infect Dis
2011
21044325
Predicting the start week of respiratory syncytial virus outbreaks using real time weather variables.
BMC Med Inform Decis Mak
2010
18694243
Forecasting hospital census at a tertiary care children's hospital.
AMIA Annu Symp Proc
2007
1 - 22 of 22
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Peter Tarczy-Hornoch
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Kenneth D Mandl
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Ingrid A Holm
Harvard Medical School
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Marta Gwinn
Rollins School of Public Health, Emory University
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Isaac S Kohane
Harvard Medical School
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Muin J Khoury
Centers for Disease Control and Prevention Atlanta GA USA.
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row(s) 1 - 30 of 30
Collaborators
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Northwestern University Feinberg School of Medicine
Co-authored papers
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University of Washington Medical Center
Co-authored papers
6
Chunhua Weng
Columbia University Irving Medical Center
Co-authored papers
6
Iftikhar J Kullo
Mayo Clinic
Co-authored papers
5
David S Carrell
Kaiser Permanente Washington Health Research Institute
Co-authored papers
4
Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers
4
Joshua C Denny
Vanderbilt University
Co-authored papers
4
Josh F Peterson
Vanderbilt University Medical Center
Co-authored papers
3
George Hripcsak
Columbia University
Co-authored papers
3
Ning Shang
Columbia University Irving Medical Center
Co-authored papers
3
Robert R Freimuth
Center for Individualized Medicine, Mayo Clinic
Co-authored papers
3
Frank D Mentch
Center for Applied Genomics (CAG), Children's Hospital of Philadelphia
Co-authored papers
3
Per H Gesteland
University of Utah School of Medicine
Co-authored papers
3
Shawn N Murphy
Harvard Medical School
Co-authored papers
3
Gail P Jarvik
University of Washington Medical Center
Co-authored papers
3
Jennifer A Pacheco
University of Pennsylvania
Co-authored papers
3
Yuan Luo
Northwestern University Feinberg School of Medicine
Co-authored papers
3
Robert J Carroll
Vanderbilt University Medical Center
Co-authored papers
3
Guilherme Del Fiol
University of Utah
Co-authored papers
3
Eric B Larson
University of Washington
Co-authored papers
3
Samuel J Aronson
Georgetown University.
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Elisabeth A Rosenthal
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Krzysztof Kiryluk
Columbia University
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Dan M Roden
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